Hirokawa M, Hashimoto Y, Ohkuma N, Mizumoto T, Iizuka H
Department of Dermatology, Asahikawa Medical College, Japan.
J Dermatol. 1990 Jul;17(7):403-8. doi: 10.1111/j.1346-8138.1990.tb01666.x.
Although calmodulin has been suggested as an important regulator of keratinocyte proliferation, its precise role remains unknown. We employed a calmodulin antagonist, N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7), to examine the role of calmodulin on keratinocyte proliferation. N-(6 aminohexyl-1-naphthalenesulfonamide (W-5), a chlorine-deficient analogue of W-7 with little anti-calmodulin activity, was used as the control. W-7 markedly inhibited thymidine incorporation of pig epidermis at concentrations close to its anti-calmodulin activity; W-5 had no effect on the thymidine incorporation. The inhibitory effect of W-7 was reversible; the removal of W-7 from the incubation medium resulted in the reinitiation of the thymidine incorporation, suggesting that W-7 is not a cytotoxic agent. These results are consistent with the view that calmodulin is an essential regulator of keratinocyte proliferation. The epidermal beta-adrenergic response, which is decreased in various hyperproliferative epidermal abnormalities, was increased in W-7-treated hypoproliferative epidermis. The epidermal SOD activity, which is also decreased in the hyperproliferative epidermis, however, was not affected by the W-7 treatment.
尽管钙调蛋白被认为是角质形成细胞增殖的重要调节因子,但其确切作用仍不清楚。我们使用钙调蛋白拮抗剂N-(6-氨基己基)-5-氯-1-萘磺酰胺(W-7)来研究钙调蛋白在角质形成细胞增殖中的作用。N-(6-氨基己基)-1-萘磺酰胺(W-5)作为对照,它是W-7的缺氯类似物,几乎没有抗钙调蛋白活性。W-7在接近其抗钙调蛋白活性的浓度下显著抑制猪表皮的胸苷掺入;W-5对胸苷掺入没有影响。W-7的抑制作用是可逆的;从孵育培养基中去除W-7会导致胸苷掺入重新开始,这表明W-7不是细胞毒性剂。这些结果与钙调蛋白是角质形成细胞增殖的必需调节因子这一观点一致。在各种增殖性表皮异常中降低的表皮β-肾上腺素能反应,在W-7处理的增殖不足的表皮中增加。然而,在增殖性表皮中也降低的表皮超氧化物歧化酶活性不受W-7处理的影响。